| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Disorders of phospholipids, sphingolipids and fatty acids biosynthesis: toward a new category of inherited metabolic diseases. | J Inherit Metab Dis | 2012 | 1.66 |
| 2 | Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1. | Neurology | 2007 | 1.13 |
| 3 | Parieto-occipital grey matter abnormalities in children with Williams syndrome. | Neuroimage | 2005 | 1.01 |
| 4 | Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. | Neurogenetics | 2009 | 0.82 |
| 5 | Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19. | Neurogenetics | 2009 | 0.81 |
| 6 | [Analgesic effects of Emla cream and saccharose solution for subcutaneous injections in preterm newborns: a prospective study of 265 injections]. | Arch Pediatr | 2004 | 0.79 |
| 7 | Clinical and genetic analysis of spinocerebellar ataxia in Mali. | Eur J Neurol | 2011 | 0.78 |